Erratum for: Choisyaternatine, a new alkaloid isolated from Choisya ternata
Published in Planta Medica 2012; 78 (14): 1597–1600
[Table 1] and the corresponding legend have been corrected.
Table 1 1H, 13C and HMBC NMR data of compound 1 (400 MHz for 1H- NMR and 100 MHz for 13C- NMR, CDCl3).
Carbon
|
δ
H (ppm)
|
δ
C (ppm)
|
DEPT
|
HMBC*
|
* Long-range 1H-13C correlation, protons to carbons of HMBC
|
1
|
|
|
C
|
|
2
|
|
160.6
|
C
|
|
3
|
6.35 (H, d, J = 9.48)
|
115.1
|
CH
|
C-2
|
4
|
7.63 (H, d, J = 9.48)
|
143.5
|
CH
|
C-2, C5
|
4a
|
|
114.4
|
C
|
|
4b
|
|
142.9
|
C
|
|
5
|
6.68 (H, s)
|
103.6
|
CH
|
C-4, C-6
|
6
|
|
150.7
|
|
|
|
3.90 (3H, s, OCH3)
|
56.3
|
CH3
|
C-6
|
7
|
|
144.9
|
C
|
|
8
|
|
141.7
|
|
|
|
4.04 (3H, s, OCH3)
|
61.7
|
CH3
|
C-8
|
1′
|
4.65 (2H, d, J = 7.28)
|
70.3
|
CH2
|
C-2′, C-3′, C-7
|
2′
|
5.57 (H, t)
|
119.9
|
CH
|
|
3′
|
|
139.3
|
C
|
|
4′
|
1.72 (3H, s, CH3)
|
25.8
|
CH3
|
C-2′, C-3′
|
5′
|
1.78 (3H, s, CH3)
|
17.9
|
CH3
|
C-2′, C-3′
|